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	<title>bomb.bio | Rob Page | Activity</title>
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				<title>Rob Page replied to the topic Implementing BOMB protocol for RNA extraction in Colombia in the forum COVID-19</title>
				<link>https://bomb.bio/forums/topic/implementing-bomb-protocol-for-rna-extraction-in-colombia/#post-9396</link>
				<pubDate>Wed, 20 May 2020 20:01:12 +1200</pubDate>

									<content:encoded><![CDATA[<p>Thank you very much for your reply Alejandro. It&#8217;s interesting that Proteinase K 10 mins @ 60 degrees should make a difference to the RdRP CT and not the RNaseP. Do you think it is simply breaking down the mucus/proteins to make the RNA more accessible to the beads? I will give it a go with our protocols tomorrow and let you (and everyone else&hellip;<span class="activity-read-more" id="activity-read-more-4687"><a href="https://bomb.bio/forums/topic/implementing-bomb-protocol-for-rna-extraction-in-colombia/#post-9396" rel="nofollow ugc">Read more</a></span></p>
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				<title>Rob Page replied to the topic Implementing BOMB protocol for RNA extraction in Colombia in the forum COVID-19</title>
				<link>https://bomb.bio/forums/topic/implementing-bomb-protocol-for-rna-extraction-in-colombia/#post-9394</link>
				<pubDate>Wed, 20 May 2020 14:53:20 +1200</pubDate>

									<content:encoded><![CDATA[<p>Hi Alejandro,</p>
<p>I am working at King&#8217;s College London and Guy&#8217;s Hosptial to set up and validate as many RNA extraction protocols for SARS-CoV-2 as possible, including several silica based methods we have developed in house. We are seeing the same thing as you described. When compared to commercial kits, our RNaseP CTs are exactly the same, but we&hellip;<span class="activity-read-more" id="activity-read-more-4685"><a href="https://bomb.bio/forums/topic/implementing-bomb-protocol-for-rna-extraction-in-colombia/#post-9394" rel="nofollow ugc">Read more</a></span></p>
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				<title>Rob Page replied to the topic  in the forum Hillbilly Bead Viral RNA Extraction Protocol - BOMB Community</title>
				<link>https://bomb.bio/forums/reply/8992/#post-8995</link>
				<pubDate>Wed, 01 Apr 2020 11:58:40 +1200</pubDate>

									<content:encoded><![CDATA[<p>Thank you so much for sharing your protocol and I&#8217;m glad to hear it worked with the spiked in RNA control. Similar to you, we have access to samples that have already been tested with commercial kits in diagnostic labs. We will compare and feedback here how it goes.</p>
<p>For the inactivation, we cannot propagate the virus in our lab but have a&hellip;<span class="activity-read-more" id="activity-read-more-4486"><a href="https://bomb.bio/forums/reply/8992/#post-8995" rel="nofollow ugc">Read more</a></span></p>
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				<title>Rob Page replied to the topic  in the forum Adjusting BOMB protocol # 8.2 for SARS-CoV-2 extraction</title>
				<link>https://bomb.bio/forums/reply/8989/#post-8991</link>
				<pubDate>Tue, 31 Mar 2020 15:23:02 +1200</pubDate>

									<content:encoded><![CDATA[<p>Hi,</p>
<p>I am also working on COVID19 diagnostics, based in London. We are going to try to use the GITC lysis RNA extraction protocol on our samples because sourcing commercial kits is starting to become a serious issue. If we can make our own then hopefully that would be much better!</p>
<p>I wondered what volume of lysis buffer you would recommend adding&hellip;<span class="activity-read-more" id="activity-read-more-4479"><a href="https://bomb.bio/forums/reply/8989/#post-8991" rel="nofollow ugc">Read more</a></span></p>
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				<title>Rob Page became a registered member</title>
				<link>https://bomb.bio/activity/p/4477/</link>
				<pubDate>Tue, 31 Mar 2020 15:09:22 +1200</pubDate>

				
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